Canonical Allele Identifier: CA1148467082

Gene: TBX19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168293282_168293285delinsAGAG , CM000663.2:g.168293282_168293285delinsAGAG	GRCh38
NC_000001.10:g.168262520_168262523delinsAGAG , CM000663.1:g.168262520_168262523delinsAGAG	GRCh37
NC_000001.9:g.166529144_166529147delinsAGAG	NCBI36
NG_008244.1:g.17243_17246delinsAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367821.8:c.603+4_603+7delinsAGAG MANE Select	ENSP00000356795.3:n.603+4_603+7delinsAGAG
ENST00000367821.7:c.603+4_603+7delinsAGAG	ENSP00000356795.3:n.603+4_603+7delinsAGAG
ENST00000431969.5:c.400+4_400+7delinsAGAG
NM_005149.2:c.603+4_603+7delinsAGAG	NP_005140.1:n.603+4_603+7delinsAGAG
NM_005149.3:c.603+4_603+7delinsAGAG MANE Select	NP_005140.1:n.603+4_603+7delinsAGAG